Title : Pre-clinical evaluation of cinobufotalin as a potential anti-lung cancer agent.

Pub. Date : 2014 Sep 26

PMID : 25201730






5 Functional Relationships(s)
Download
Sentence
Compound Name
Protein Name
Organism
1 Our data suggest that mitochondrial protein cyclophilin D (Cyp-D)-dependent mitochondrial permeability transition pore (mPTP) opening mediates cinobufotalin-induced non-apoptotic death of lung cancer cells. cinobufotalin peptidylprolyl isomerase F (cyclophilin F) Mus musculus
2 Our data suggest that mitochondrial protein cyclophilin D (Cyp-D)-dependent mitochondrial permeability transition pore (mPTP) opening mediates cinobufotalin-induced non-apoptotic death of lung cancer cells. cinobufotalin peptidylprolyl isomerase F (cyclophilin F) Mus musculus
3 The Cyp-D inhibitor cyclosporine A (CsA), the mPTP blocker sanglifehrin A (SfA), and Cyp-D shRNA-silencing significantly inhibited cinobufotalin-induced mitochondrial membrane potential (MMP) reduction and A549 cell death (but not apoptosis). cinobufotalin peptidylprolyl isomerase F (cyclophilin F) Mus musculus
4 The Cyp-D inhibitor cyclosporine A (CsA), the mPTP blocker sanglifehrin A (SfA), and Cyp-D shRNA-silencing significantly inhibited cinobufotalin-induced mitochondrial membrane potential (MMP) reduction and A549 cell death (but not apoptosis). cinobufotalin peptidylprolyl isomerase F (cyclophilin F) Mus musculus
5 Thus, cinobufotalin mainly induces Cyp-D-dependent non-apoptotic death in cultured lung cancer cells. cinobufotalin peptidylprolyl isomerase F (cyclophilin F) Mus musculus